Optimal plasma progranulin cutoff value for predicting null progranulin mutations in neurodegenerative diseases: a multicenter Italian study (Q50980787)

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scientific article published on 26 November 2011

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English	Optimal plasma progranulin cutoff value for predicting null progranulin mutations in neurodegenerative diseases: a multicenter Italian study	scientific article published on 26 November 2011

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Europe PubMed Central

PubMed publication ID

22123177

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26 March 2018

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http://europepmc.org/abstract/MED/22123177

title

Optimal plasma progranulin cutoff value for predicting null progranulin mutations in neurodegenerative diseases: a multicenter Italian study (English)

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Europe PubMed Central

PubMed publication ID

22123177

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26 March 2018

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http://europepmc.org/abstract/MED/22123177

main subject

Italy

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neurodegeneration

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author

Roberta Ghidoni

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1

1 reference

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Europe PubMed Central

PubMed publication ID

22123177

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26 March 2018

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http://europepmc.org/abstract/MED/22123177

Elio Scarpini

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11

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PubMed publication ID

22123177

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26 March 2018

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http://europepmc.org/abstract/MED/22123177

Daniela Galimberti

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12

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Europe PubMed Central

PubMed publication ID

22123177

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26 March 2018

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http://europepmc.org/abstract/MED/22123177

Michela Morbin

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13

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PubMed publication ID

22123177

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26 March 2018

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http://europepmc.org/abstract/MED/22123177

Luisa Benussi

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16

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PubMed publication ID

22123177

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26 March 2018

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http://europepmc.org/abstract/MED/22123177

Anna Paterlini

object named as

Anna Paterlini

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6

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Fabrizio Tagliavini

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Fabrizio Tagliavini

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14

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Chiara Fenoglio

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10

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Chiara Fenoglio

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Europe PubMed Central

PubMed publication ID

22123177

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26 March 2018

reference URL

http://europepmc.org/abstract/MED/22123177

Luigi Francesco Agnati

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9

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Luigi F Agnati

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PubMed publication ID

22123177

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26 March 2018

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http://europepmc.org/abstract/MED/22123177

Eleonora Pegoiani

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8

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Eleonora Pegoiani

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Europe PubMed Central

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22123177

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26 March 2018

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http://europepmc.org/abstract/MED/22123177

Valentina Albertini

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5

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Valentina Albertini

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Europe PubMed Central

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22123177

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26 March 2018

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http://europepmc.org/abstract/MED/22123177

Elena Stoppani

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2

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Elena Stoppani

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22123177

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26 March 2018

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http://europepmc.org/abstract/MED/22123177

Michela Glionna

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7

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Michela Glionna

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Europe PubMed Central

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22123177

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26 March 2018

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http://europepmc.org/abstract/MED/22123177

Giacomina Rossi

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3

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Giacomina Rossi

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Europe PubMed Central

PubMed publication ID

22123177

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26 March 2018

reference URL

http://europepmc.org/abstract/MED/22123177

Giuliano Binetti

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15

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Giuliano Binetti

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Europe PubMed Central

PubMed publication ID

22123177

retrieved

26 March 2018

reference URL

http://europepmc.org/abstract/MED/22123177

Elena Piccoli

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4

object named as

Elena Piccoli

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Europe PubMed Central

PubMed publication ID

22123177

retrieved

26 March 2018

reference URL

http://europepmc.org/abstract/MED/22123177

publication date

26 November 2011

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Europe PubMed Central

PubMed publication ID

22123177

retrieved

26 March 2018

reference URL

http://europepmc.org/abstract/MED/22123177

published in

Neurodegenerative Diseases

1 reference

stated in

Europe PubMed Central

PubMed publication ID

22123177

retrieved

26 March 2018

reference URL

http://europepmc.org/abstract/MED/22123177

volume

9

1 reference

stated in

Europe PubMed Central

PubMed publication ID

22123177

retrieved

26 March 2018

reference URL

http://europepmc.org/abstract/MED/22123177

issue

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

22123177

retrieved

26 March 2018

reference URL

http://europepmc.org/abstract/MED/22123177

page(s)

121-127

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Europe PubMed Central

PubMed publication ID

22123177

retrieved

26 March 2018

reference URL

http://europepmc.org/abstract/MED/22123177

cites work

Frontotemporal dementia.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1159%2F000333132

retrieved

21 January 2018

Molecular pathways of frontotemporal lobar degeneration

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1159%2F000333132

retrieved

21 January 2018

Clinical, genetic and pathological heterogeneity of frontotemporal dementia: a review

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1159%2F000333132

retrieved

21 January 2018

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1159%2F000333132

retrieved

21 January 2018

Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1159%2F000333132

retrieved

21 January 2018

Progranulin Mutations are a Common Cause of FTLD in Northern Italy

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1159%2F000333132

retrieved

21 January 2018

Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1159%2F000333132

retrieved

21 January 2018

Mutations in progranulin (GRN) within the spectrum of clinical and pathological phenotypes of frontotemporal dementia

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1159%2F000333132

retrieved

21 January 2018

Low plasma progranulin levels predict progranulin mutations in frontotemporal lobar degeneration.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1159%2F000333132

retrieved

21 January 2018

Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1159%2F000333132

retrieved

21 January 2018

Mild cognitive impairment: clinical characterization and outcome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1159%2F000333132

retrieved

21 January 2018

A novel deletion in progranulin gene is associated with FTDP-17 and CBS.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1159%2F000333132

retrieved

21 January 2018

Progranulin Leu271LeufsX10 is one of the most common FTLD and CBS associated mutations worldwide.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1159%2F000333132

retrieved

21 January 2018

Progranulin plasma levels as potential biomarker for the identification of GRN deletion carriers. A case with atypical onset as clinical amnestic Mild Cognitive Impairment converted to Alzheimer's disease

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1159%2F000333132

retrieved

21 January 2018

Serum biomarker for progranulin-associated frontotemporal lobar degeneration

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1159%2F000333132

retrieved

21 January 2018

TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriers.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1159%2F000333132

retrieved

21 January 2018

An algorithm for genetic testing of frontotemporal lobar degeneration

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1159%2F000333132

retrieved

21 January 2018

Identifiers

DOI

10.1159/000333132

1 reference

stated in

Europe PubMed Central

PubMed publication ID

22123177

retrieved

26 March 2018

reference URL

http://europepmc.org/abstract/MED/22123177

PubMed publication ID

22123177

1 reference

stated in

Europe PubMed Central

PubMed publication ID

22123177

retrieved

26 March 2018

reference URL

http://europepmc.org/abstract/MED/22123177

 

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